Variant report

Variant	esv2756137
Chromosome Location	chr7:124521049-124558049
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:148)
CpG islands
(count:122)
Chromatin interactive
region (count:22)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:148 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr7:124547598-124547886	K562	blood:	n/a	n/a
2	ATF2	chr7:124533127-124533673	GM12878	blood:	n/a	n/a
3	ATF2	chr7:124533021-124534035	GM12878	blood:	n/a	n/a
4	BATF	chr7:124533246-124533843	GM12878	blood:	n/a	chr7:124533362-124533372
5	BATF	chr7:124533179-124533530	GM12878	blood:	n/a	chr7:124533362-124533372
6	BCL11A	chr7:124533121-124533611	GM12878	blood:	n/a	n/a
7	BCL3	chr7:124533131-124533577	GM12878	blood:	n/a	n/a
8	BCLAF1	chr7:124533247-124533646	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:124554502-124554557	GM12878	blood:	n/a	n/a
10	CEBPB	chr7:124522033-124522372	K562	blood:	n/a	chr7:124522229-124522240 chr7:124522094-124522107 chr7:124522094-124522107 chr7:124522227-124522240 chr7:124522229-124522238
11	CEBPB	chr7:124533035-124534036	GM12878	blood:	n/a	n/a
12	CEBPB	chr7:124528270-124528553	HepG2	liver:	n/a	n/a
13	CEBPB	chr7:124528252-124528469	K562	blood:	n/a	n/a
14	CEBPB	chr7:124522078-124522422	HepG2	liver:	n/a	chr7:124522229-124522240 chr7:124522094-124522107 chr7:124522094-124522107 chr7:124522227-124522240 chr7:124522229-124522238
15	CTCF	chr7:124522239-124522436	K562	blood:	n/a	n/a
16	CTCF	chr7:124527201-124527225	GM13976	blood:	n/a	n/a
17	CTCF	chr7:124541294-124541326	Lung_OC	lung:	n/a	n/a
18	CTCF	chr7:124546245-124546280	GM13977	blood:	n/a	n/a
19	CUX1	chr7:124554439-124554621	GM12878	blood:	n/a	n/a
20	CUX1	chr7:124536969-124537169	K562	blood:	n/a	chr7:124537018-124537027
21	EBF1	chr7:124556765-124556934	GM12878	blood:	n/a	n/a
22	EP300	chr7:124533214-124533732	GM12878	blood:	n/a	chr7:124533307-124533321
23	EP300	chr7:124533191-124533586	GM12878	blood:	n/a	chr7:124533307-124533321
24	FOS	chr7:124548350-124548589	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr7:124525132-124525274	MCF10A-Er-Src	breast:	n/a	chr7:124525202-124525211 chr7:124525202-124525210 chr7:124525203-124525210 chr7:124525201-124525210
26	FOS	chr7:124548362-124548560	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr7:124525140-124525346	MCF10A-Er-Src	breast:	n/a	chr7:124525202-124525211 chr7:124525202-124525210 chr7:124525203-124525210 chr7:124525201-124525210
28	FOXM1	chr7:124533033-124533660	GM12878	blood:	n/a	n/a
29	FOXM1	chr7:124533063-124533864	GM12878	blood:	n/a	n/a
30	GATA3	chr7:124551485-124551734	SH-SY5Y	brain:	n/a	chr7:124551537-124551546
31	GATA3	chr7:124550459-124550499	SH-SY5Y	brain:	n/a	n/a
32	GATA3	chr7:124534688-124534797	SH-SY5Y	brain:	n/a	chr7:124534744-124534752
33	GATA3	chr7:124537483-124537550	SH-SY5Y	brain:	n/a	n/a
34	HCFC1	chr7:124527216-124527301	K562	blood:	n/a	n/a
35	IKZF1	chr7:124533189-124533820	GM12878	blood:	n/a	n/a
36	IRF1	chr7:124547685-124547796	K562	blood:	n/a	n/a
37	IRF1	chr7:124549045-124549062	K562	blood:	n/a	n/a
38	IRF1	chr7:124551630-124551634	K562	blood:	n/a	n/a
39	IRF1	chr7:124539465-124539758	K562	blood:	n/a	chr7:124539614-124539626 chr7:124539615-124539625
40	IRF3	chr7:124538643-124538744	GM12878	blood:	n/a	n/a
41	IRF4	chr7:124533094-124533823	GM12878	blood:	n/a	n/a
42	JUN	chr7:124527369-124527680	K562	blood:	n/a	n/a
43	JUN	chr7:124525133-124525260	HepG2	liver:	n/a	chr7:124525202-124525211 chr7:124525202-124525210 chr7:124525203-124525210 chr7:124525201-124525210
44	JUN	chr7:124522250-124522483	K562	blood:	n/a	n/a
45	JUND	chr7:124533202-124533552	GM12878	blood:	n/a	chr7:124533385-124533393 chr7:124533386-124533393
46	JUND	chr7:124547594-124547844	HepG2	liver:	n/a	n/a
47	JUND	chr7:124525042-124525333	HepG2	liver:	n/a	chr7:124525202-124525211 chr7:124525200-124525211 chr7:124525202-124525210 chr7:124525203-124525210 chr7:124525201-124525210
48	KAP1	chr7:124555083-124555431	K562	blood:	n/a	n/a
49	KAP1	chr7:124531691-124531935	K562	blood:	n/a	n/a
50	KAP1	chr7:124530504-124530732	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:124538660-124538710	HRCEpiC	kidney:	n/a
2	chr7:124536676-124536726	HMEC	breast:	n/a
3	chr7:124536676-124536726	BJ	skin:	n/a
4	chr7:124536676-124536726	Hela-S3	cervix:	n/a
5	chr7:124538660-124538710	CMK	blood:	n/a
6	chr7:124536676-124536726	PrEC	prostate:	n/a
7	chr7:124538660-124538710	HEEpiC	esophagus:	n/a
8	chr7:124538660-124538710	MCF10A-Er-Src	breast:	n/a
9	chr7:124536676-124536726	SK-N-MC	brain:	n/a
10	chr7:124538660-124538710	RPTEC	kidney:	n/a
11	chr7:124538660-124538710	NH-A	brain:	n/a
12	chr7:124536676-124536726	HCF	heart:	n/a
13	chr7:124536676-124536726	H1-hESC	embryonic stem cell:	embryo
14	chr7:124536676-124536726	T-47D	breast:	n/a
15	chr7:124538660-124538710	AG04449	skin:	fetal
16	chr7:124538660-124538710	SK-N-SH	brain:	n/a
17	chr7:124538660-124538710	HCT-116	colon:	n/a
18	chr7:124536676-124536726	AG09309	skin:	n/a
19	chr7:124538660-124538710	ovcar-3	ovarian:	n/a
20	chr7:124536676-124536726	MCF-7	breast:	n/a
21	chr7:124538660-124538710	HRE	kidney:	n/a
22	chr7:124538660-124538710	SK-N-SH_RA	brain:	n/a
23	chr7:124538660-124538710	ProgFib	skin:	n/a
24	chr7:124536676-124536726	SK-N-SH_RA	brain:	n/a
25	chr7:124538660-124538710	HCPEpiC	choroid plexus:	n/a
26	chr7:124538660-124538710	Caco-2	colon:	n/a
27	chr7:124536676-124536726	HEEpiC	esophagus:	n/a
28	chr7:124536676-124536726	NB4	blood:	n/a
29	chr7:124538660-124538710	T-47D	breast:	n/a
30	chr7:124536676-124536726	GM12878	blood:	n/a
31	chr7:124538660-124538710	SK-N-MC	brain:	n/a
32	chr7:124538660-124538710	NHBE	bronchial:	n/a
33	chr7:124538660-124538710	GM19239	blood:	n/a
34	chr7:124536676-124536726	IMR90	lung:	fetal
35	chr7:124536676-124536726	A549	lung:	n/a
36	chr7:124536676-124536726	HCPEpiC	choroid plexus:	n/a
37	chr7:124536676-124536726	HIPEpiC	eye:	n/a
38	chr7:124538660-124538710	Hela-S3	cervix:	n/a
39	chr7:124536676-124536726	GM19239	blood:	n/a
40	chr7:124538660-124538710	Hepatocyte	liver:	n/a
41	chr7:124536676-124536726	HRE	kidney:	n/a
42	chr7:124536676-124536726	HRCEpiC	kidney:	n/a
43	chr7:124536676-124536726	HCM	heart:	n/a
44	chr7:124536676-124536726	Hepatocyte	liver:	n/a
45	chr7:124538660-124538710	NT2-D1	testis:	n/a
46	chr7:124536676-124536726	Jurkat	blood:	n/a
47	chr7:124538660-124538710	GM12892	blood:	n/a
48	chr7:124536676-124536726	ProgFib	skin:	n/a
49	chr7:124536676-124536726	PFSK-1	brain:	n/a
50	chr7:124538660-124538710	NB4	blood:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:124549176..124550827-chr7:124558825..124561252,2	K562	blood:
2	chr7:124523248..124524832-chr7:124524843..124527299,2	K562	blood:
3	chr7:124551396..124553692-chr7:124554817..124557525,2	K562	blood:
4	chr7:124557098..124558767-chr7:124568438..124571328,3	K562	blood:
5	chr7:124546480..124548936-chr7:124561383..124564382,2	K562	blood:
6	chr7:124514345..124516702-chr7:124522638..124525470,2	K562	blood:
7	chr7:124509328..124512200-chr7:124525165..124526701,2	K562	blood:
8	chr7:124523515..124526179-chr7:124527945..124529532,2	MCF-7	breast:
9	chr7:124518995..124522486-chr7:124524978..124527724,3	K562	blood:
10	chr7:124534351..124537236-chr7:124567413..124569702,2	K562	blood:
11	chr7:124522245..124524955-chr7:124533723..124536178,2	K562	blood:
12	chr7:124537777..124539651-chr7:124561497..124564089,2	K562	blood:
13	chr7:124523248..124524832-chr7:124524843..124527299,2	K562	blood:
14	chr7:124520545..124522828-chr7:124555215..124557862,2	K562	blood:
15	chr7:124550905..124554322-chr7:124566903..124570128,4	K562	blood:
16	chr7:124518995..124522486-chr7:124524978..124527724,3	K562	blood:
17	chr7:124522245..124524955-chr7:124533723..124536178,2	K562	blood:
18	chr7:124523515..124526179-chr7:124527945..124529532,2	MCF-7	breast:
19	chr7:124521370..124523136-chr7:124567552..124569550,2	K562	blood:
20	chr7:124551396..124553692-chr7:124554817..124557525,2	K562	blood:
21	chr7:124520545..124522828-chr7:124555215..124557862,2	K562	blood:
22	chr7:124524737..124527454-chr7:124559196..124561248,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR37-2	chr7:124538315-124538428	NONHSAT123087
2	lnc-GPR37-2	chr7:124555628-124555700	NONHSAT123087

No data

Variant related genes	Relation type
POT1	TF binding region
POT1	CpG island
ENSG00000128513	chromatin interactions
ENSG00000224897	chromatin interactions

Extended variants
information (count: 1280 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1280 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370908940	chr7:124521062-124521063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs191422081	chr7:124521104-124521105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141032821	chr7:124521120-124521121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs570094731	chr7:124521123-124521124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs7796015	chr7:124521146-124521147	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs553957386	chr7:124521160-124521161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs184515432	chr7:124521199-124521200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565955724	chr7:124521215-124521216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7796150	chr7:124521217-124521218	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs558121164	chr7:124521238-124521239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577761405	chr7:124521240-124521241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536897279	chr7:124521247-124521248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188994235	chr7:124521327-124521328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370368695	chr7:124521339-124521340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573664665	chr7:124521365-124521366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7799938	chr7:124521391-124521392	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs574524848	chr7:124521427-124521428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs10226033	chr7:124521430-124521431	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs531342719	chr7:124521431-124521432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541821227	chr7:124521525-124521526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs147936727	chr7:124521620-124521621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564479192	chr7:124521718-124521719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs12530981	chr7:124521722-124521723	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs371072903	chr7:124521747-124521748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs543655435	chr7:124521799-124521800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563759124	chr7:124521802-124521803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529393752	chr7:124521859-124521860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549529422	chr7:124521860-124521861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548088756	chr7:124521904-124521905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs193127440	chr7:124521911-124521912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528537520	chr7:124521930-124521931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139526394	chr7:124521951-124521952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571456123	chr7:124521959-124521960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537210179	chr7:124521990-124521991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs556892578	chr7:124522067-124522068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs145164589	chr7:124522168-124522169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185774500	chr7:124522171-124522172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs144880198	chr7:124522230-124522231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs572494722	chr7:124522263-124522264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544649301	chr7:124522287-124522288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557980812	chr7:124522331-124522332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs578192445	chr7:124522337-124522338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188800272	chr7:124522350-124522351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563710846	chr7:124522356-124522357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181574347	chr7:124522407-124522408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs149044760	chr7:124522443-124522444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183805790	chr7:124522470-124522471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552605624	chr7:124522493-124522494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528448673	chr7:124522527-124522528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs188722674	chr7:124522533-124522534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	21635232	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myxofibrosarcoma	20639860	CNVD

Chromatin state (count:501 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:124461400-124530800	Weak transcription	NHDF-Ad	bronchial
2	chr7:124462200-124568200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr7:124464600-124530600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr7:124466400-124540800	Weak transcription	Right Ventricle	heart
5	chr7:124466400-124562200	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr7:124466600-124563400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr7:124466800-124540800	Weak transcription	Gastric	stomach
8	chr7:124467600-124530600	Weak transcription	NH-A	brain
9	chr7:124477000-124530800	Weak transcription	Primary B cells from peripheral blood	blood
10	chr7:124484200-124554400	Weak transcription	HUVEC	blood vessel
11	chr7:124487200-124534800	Weak transcription	Fetal Heart	heart
12	chr7:124488400-124531200	Weak transcription	Osteobl	bone
13	chr7:124490800-124540600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr7:124498000-124529000	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr7:124498200-124568800	Weak transcription	Brain Anterior Caudate	brain
16	chr7:124502200-124528800	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr7:124503000-124531000	Weak transcription	GM12878-XiMat	blood
18	chr7:124503600-124528600	Weak transcription	Liver	Liver
19	chr7:124503800-124528600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr7:124503800-124529000	Weak transcription	Adipose Nuclei	Adipose
21	chr7:124503800-124529200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr7:124503800-124529400	Weak transcription	Left Ventricle	heart
23	chr7:124504200-124529200	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr7:124504200-124530400	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr7:124505600-124531000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr7:124506600-124540600	Weak transcription	Aorta	Aorta
27	chr7:124506800-124527600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr7:124506800-124540600	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr7:124507000-124528200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr7:124507000-124528600	Weak transcription	Primary B cells from cord blood	blood
31	chr7:124507000-124529400	Weak transcription	Fetal Muscle Leg	muscle
32	chr7:124507200-124528800	Weak transcription	Primary T cells from cord blood	blood
33	chr7:124507200-124529000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr7:124507200-124529000	Weak transcription	Fetal Lung	lung
35	chr7:124507200-124529200	Weak transcription	HSMM	muscle
36	chr7:124507200-124531000	Weak transcription	K562	blood
37	chr7:124507400-124529000	Weak transcription	Primary hematopoietic stem cells	blood
38	chr7:124507600-124528600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr7:124507600-124528600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr7:124507600-124528600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr7:124507600-124529200	Weak transcription	Ovary	ovary
42	chr7:124508000-124529000	Weak transcription	Dnd41	blood
43	chr7:124516800-124522400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr7:124518000-124535200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
45	chr7:124519200-124530600	Weak transcription	Fetal Thymus	thymus
46	chr7:124520200-124531000	Weak transcription	Brain Angular Gyrus	brain
47	chr7:124520200-124534400	Weak transcription	Brain Hippocampus Middle	brain
48	chr7:124520400-124534600	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr7:124520400-124534800	Weak transcription	Brain Substantia Nigra	brain
50	chr7:124521600-124521800	Enhancers	HUES64 Cell Line	embryonic stem cell

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